Publication:
29-Deoxymaklamicin, a new maklamicin analogue produced by a genetically engineered strain of Micromonospora sp. NBRC 110955

dc.contributor.authorRatama Daduangen_US
dc.contributor.authorShigeru Kitanien_US
dc.contributor.authorYuri Sudohen_US
dc.contributor.authorIvy Grace Umadhay Paiten_US
dc.contributor.authorArinthip Thamchaipeneten_US
dc.contributor.authorHaruo Ikedaen_US
dc.contributor.authorYasuhiro Igarashien_US
dc.contributor.authorTakuya Nihiraen_US
dc.contributor.otherOsaka Universityen_US
dc.contributor.otherHyphagenesis Inc.en_US
dc.contributor.otherKasetsart Universityen_US
dc.contributor.otherKitasato Universityen_US
dc.contributor.otherToyama Prefectural Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-11-23T09:36:33Z
dc.date.available2018-11-23T09:36:33Z
dc.date.issued2015-12-01en_US
dc.description.abstract© 2015 The Society for Biotechnology, Japan. Maklamicin is a spirotetronate-class antibiotic produced by Micromonospora sp. NBRC 110955, and a polyketide assembly line and a glycerate utilization system are involved in its biosynthesis. One tailoring step in the biosynthesis is predicted to be post-polyketide synthase (PKS) modification, which seems to be catalysed by putative cytochrome P450 monooxygenases, MakC2 and/or MakC3. In this study, we characterized makC2 and makC3 in the biosynthesis of maklamicin and identified a new maklamicin analogue from a makC2 disruptant. Gene deletion of makC2 resulted in the complete loss of maklamicin production with concomitant accumulation of a new compound (29-deoxymaklamicin), while gene deletion of makC3 did not affect the maklamicin production, indicating that 29-deoxymaklamicin is an intermediate in the biosynthetic pathway of maklamicin and should serve as the substrate of MakC2. 29-Deoxymaklamicin showed strong-to-modest anti-microbial activity against gram-positive bacteria. The fact that Streptomyces avermitilis heterologously expressing makC2 successfully converted 29-deoxymaklamicin into maklamicin confirmed that MakC2 is the final-step hydroxylase in the formation of mature maklamicin.en_US
dc.identifier.citationJournal of Bioscience and Bioengineering. Vol.120, No.6 (2015), 608-613en_US
dc.identifier.doi10.1016/j.jbiosc.2015.04.004en_US
dc.identifier.issn13474421en_US
dc.identifier.issn13891723en_US
dc.identifier.other2-s2.0-84946486196en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/35344
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84946486196&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemical Engineeringen_US
dc.subjectImmunology and Microbiologyen_US
dc.title29-Deoxymaklamicin, a new maklamicin analogue produced by a genetically engineered strain of Micromonospora sp. NBRC 110955en_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84946486196&origin=inwarden_US

Files

Collections